CorticaLINK Spinal Fusion Platform

CorticaLINK Spinal Fusion Platform is an FDA 510(k)-cleared medical device (K160722) manufactured by Facetlink Dba Linkspine. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 6, 2016. Regulation: 8.